Canonical Allele Identifier: CA1522520349
Gene: SLC6A19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213553G= , CM000667.2:g.1213553G= GRCh38
NC_000005.9:g.1213668G= , CM000667.1:g.1213668G= GRCh37
NC_000005.8:g.1266668G= NCBI36
NG_008282.1:g.16959G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.754G= MANE Select ENSP00000305302.10:p.Val252=
ENST00000304460.10:c.754G= ENSP00000305302.10:p.Val252=
ENST00000515652.5:c.662G= ENSP00000425701.1:p.Arg221=
NM_001003841.2:c.754G= NP_001003841.1:p.Val252=
NM_001003841.3:c.754G= MANE Select NP_001003841.1:p.Val252=